| C0011195 |
Dejerine-Sottas Disease (disorder) |
DO |
Charcot-Marie-Tooth disease dominant intermediate F
|
0110206 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
DO |
Charcot-Marie-Tooth disease X-linked dominant 6
|
0110207 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
DO |
Charcot-Marie-Tooth disease X-linked recessive 2
|
0110208 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
DO |
Charcot-Marie-Tooth disease X-linked dominant 1
|
0110209 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
DO |
Charcot-Marie-Tooth disease X-linked recessive 5
|
0110210 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
DO |
Charcot-Marie-Tooth disease X-linked recessive 3
|
0110211 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
DO |
Charcot-Marie-Tooth disease X-linked recessive 4
|
0110212 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
DO |
Charcot-Marie-Tooth disease
|
10595 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
DO |
motor peripheral neuropathy
|
2477 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
EFO |
charcot-marie-tooth disease, axonal, type 2t
|
0009162 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
ICD10CM |
Charcot-Marie-Tooth disease
|
G60.0 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
ICD10CM |
Déjérine-Sottas disease
|
G60.0 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
ICD10CM |
Hereditary motor and sensory neuropathy
|
G60.0 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
ICD10CM |
Roussy-Levy syndrome
|
G60.0 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
ICD10CM |
Hypertrophic neuropathy of infancy
|
G60.0 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
ICD10CM |
Hereditary motor and sensory neuropathy, types I-IV
|
G60.0 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
ICD10CM |
Peroneal muscular atrophy (axonal type) (hypertrophic type)
|
G60.0 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
MONDO |
agenesis of the corpus callosum with peripheral neuropathy
|
0000902 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
MONDO |
Charcot-Marie-Tooth disease type 1B
|
0007307 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
MONDO |
Charcot-Marie-Tooth disease type 2A1
|
0007308 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
MONDO |
Charcot-Marie-Tooth disease type 1A
|
0007309 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
MONDO |
Charcot-Marie-Tooth disease type 1E
|
0007311 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
MONDO |
Charcot-Marie-Tooth disease type 3
|
0007790 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
MONDO |
Charcot-Marie-Tooth disease type 4A
|
0008961 |
| C0011195 |
Dejerine-Sottas Disease (disorder) |
MONDO |
Charcot-Marie-Tooth disease X-linked dominant 6
|
0010479 |